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[Federal Register: August 26, 2008 (Volume 73, Number 166)]
[
Notices]
[Page 50331-50332]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr26au08-70]
[[Page 50331]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-08-08BM]
Proposed Data Collections Submitted for Public Comment and
Recommendations
In compliance with the requirement of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for opportunity for public comment on
proposed data collection projects, the Centers for Disease Control and
Prevention (CDC) will publish periodic summaries of proposed projects.
To request more information on the proposed projects or to obtain a
copy of the data collection plans and instruments, call 404-639-5960
and send comments to Maryam I. Daneshvar, CDC Acting Reports Clearance
Officer, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail
to omb@cdc.gov.
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (b) the accuracy of the agency's estimate of the burden of the
proposed collection of information; (c) ways to enhance the quality,
utility, and clarity of the information to be collected; and (d) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques or other
forms of information technology. Written comments should be received
within 60 days of this notice.
Proposed Project
An Examination of the Implementation of the Safe Dates Program
Under Naturalistic Conditions--New--National Center for Injury
Prevention and Control (NCIPC), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The specific aims of this study are to conduct a survey that will
allow for a greater understanding of the implementation of the Safe
Dates program in a real-world context among parties that purchase the
curriculum directly from the publisher (Hazelden Foundation), to
describe circumstances leading up to the purchase decision, to examine
the extent to which the program is implemented as designed and tested
(i.e., with fidelity), and to identify circumstances that support or
hinder high-fidelity implementation of this evidence-based dating
violence prevention program. The proposed study presents a unique
opportunity to directly gather information from curriculum purchasers
and program implementers who typically are not involved in
implementation research but who are likely to represent real-world
implementers of evidence-based curricula.
There is an increasing trend for publishing houses to buy the
rights to evidence-based curricula directly from the developer.
However, little information exists to determine whether or not those
who purchase the curricula implement it as intended. If not, then
program benefits may not be achieved. This project will allow CDC to
determine whether or not one evidence-based program, Safe Dates, is
implemented as intended, and will inform CDC's efforts to facilitate
the widespread but effective implementation of evidence-based
curricula.
With support from the publishing company, the investigation will
seek participation from an estimated 1,000 organizations and/or
individuals who purchased the curriculum and who know about how it was
implemented. A particular focus will be placed on investigating the
extent to which the program, which includes 9 classroom sessions, a
play, and a poster contest, was implemented with fidelity. This is
important given that there is no evidence of program effectiveness if
less than the full curriculum is delivered.
All data will be collected through Web-based questionnaires. The
design of these questionnaires is informed by a theoretical model
grounded in the organizational behavior, psychology and healthcare
planning literatures that illuminates factors and processes expected to
impact the decision to implement evidence-based programs and, also, the
extent to which these programs are implemented with fidelity.
Consequently, items included in the Web questionnaires are adapted from
existing scales with known reliability. The questionnaires will include
a section on characteristics of the purchasing organization, factors
that lead to the decision to purchase the curriculum, and questions
related to whether the program was implemented as intended.
A snowball sampling technique will be used to recruit survey
respondents. First, an initial letter on CDC letterhead will be sent by
the publisher to roughly 1,000 individuals known to have purchased the
curriculum. This information is available from a mailing list kept by
the publisher. Second, individuals on the mailing list will be asked to
complete the survey and to provide contact information for other
individuals known to have implemented the curriculum. And third, these
individuals will be asked to complete the survey and provide other
relevant contacts. The survey and lead letter will state on the opening
screen that participation in the study is voluntary. Informed consent
will be obtained from all participants prior to completing the surveys.
Roughly 1,000 lead letters will be mailed and it is expected 500
surveys will be completed.
There are no costs to respondents except their time to complete
surveys.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Estimated Number of Average burden Estimated total
Respondents number of responses per per response burden (in
respondents respondent (in hours) hours)
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Web-survey.................................. 500 1 27/60 225
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Total................................... ............... ............... ............... 225
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[[Page 50332]]
Dated: August 18, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E8-19728 Filed 8-25-08; 8:45 am]
BILLING CODE 4163-18-P
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